Canonical Allele Identifier: CA104789493
Gene: IL2 HGNC NCBI

Linked Data

dbSNP Id: rs2069776

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122450821A>G , CM000666.2:g.122450821A>G GRCh38
NC_000004.11:g.123371976A>G , CM000666.1:g.123371976A>G GRCh37
NC_000004.10:g.123591426A>G NCBI36
NG_016779.1:g.10675T>C

Transcript Alleles

HGVS Amino-acid change
XM_017008177.1:c.352-1262T>C XP_016863666.1:n.352-1262T>C